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Extremely High Serum Ferritin: An Instrumental Marker of Masquerading Adult-Onset Still’s Disease with Hemophagocytic Syndrome
Patient: Female, 88 Final Diagnosis: Adult onset still’s disease Symptoms: Fever • rash Medication: — Clinical Procedure: — Specialty: Rhaumatology OBJECTIVE: Unusual clinical course BACKGROUND: Adult-onset Still’s disease (AOSD) is a rare multi-systemic inflammatory disorder of unknown etiology cha...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Scientific Literature, Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726146/ https://www.ncbi.nlm.nih.gov/pubmed/29208852 http://dx.doi.org/10.12659/AJCR.905684 |
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author | Yamashita, Shun Furukawa, Naoko E. Matsunaga, Tomoyo Hirakawa, Yuka Tago, Masaki Yamashita, Shu-ichi |
author_facet | Yamashita, Shun Furukawa, Naoko E. Matsunaga, Tomoyo Hirakawa, Yuka Tago, Masaki Yamashita, Shu-ichi |
author_sort | Yamashita, Shun |
collection | PubMed |
description | Patient: Female, 88 Final Diagnosis: Adult onset still’s disease Symptoms: Fever • rash Medication: — Clinical Procedure: — Specialty: Rhaumatology OBJECTIVE: Unusual clinical course BACKGROUND: Adult-onset Still’s disease (AOSD) is a rare multi-systemic inflammatory disorder of unknown etiology characterized by spiking fever, characteristic rash, and arthritis. It often associates with high serum ferritin levels. CASE REPORT: An 88-year-old woman had fever of over 39°C without response to extended-spectrum antibiotics for 6 days. She had non-specific erythema with infiltration on her trunk. She had leukocytosis with neutrophilia of 80%, mild hepatic dysfunction, normal level of rheumatoid factor and antinuclear antibody, thrombocytopenia, elevated d-dimer and soluble interleukin2 receptor, extremely high serum ferritin (78 662 ng/mL), and splenomegaly. Although she had no arthritis or specific erythema, we made the diagnosis of AOSD according to Yamaguchi’s criteria with disseminated intravascular coagulation (DIC) and hemophagocytic syndrome (HPS) after ruling out infections, malignancies, or other connective tissue diseases. Twelve percent of AOSD patients have HPS. The mean serum ferritin of AOSD with HPS was reported at 18 179 ng/mL, which supported the diagnosis of AOSD because only a few other diseases could show such extremely high serum ferritin. Although she was treated with prednisolone (30 mg/day), her condition deteriorated and her left pleural effusion increased. Therefore, methylprednisolone 500 mg/day for 3 days was started followed by prednisolone 30 mg/day and immunosuppressive agent (Cyclosporine 50 mg/day), which improved her general condition, elevated C-reactive protein levels, and extremely high serum ferritin levels. CONCLUSIONS: We report the case of an elderly patient with severe AOSD, who developed HPS and DIC, whose extremely high serum ferritin level was useful in diagnosis. |
format | Online Article Text |
id | pubmed-5726146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57261462017-12-14 Extremely High Serum Ferritin: An Instrumental Marker of Masquerading Adult-Onset Still’s Disease with Hemophagocytic Syndrome Yamashita, Shun Furukawa, Naoko E. Matsunaga, Tomoyo Hirakawa, Yuka Tago, Masaki Yamashita, Shu-ichi Am J Case Rep Articles Patient: Female, 88 Final Diagnosis: Adult onset still’s disease Symptoms: Fever • rash Medication: — Clinical Procedure: — Specialty: Rhaumatology OBJECTIVE: Unusual clinical course BACKGROUND: Adult-onset Still’s disease (AOSD) is a rare multi-systemic inflammatory disorder of unknown etiology characterized by spiking fever, characteristic rash, and arthritis. It often associates with high serum ferritin levels. CASE REPORT: An 88-year-old woman had fever of over 39°C without response to extended-spectrum antibiotics for 6 days. She had non-specific erythema with infiltration on her trunk. She had leukocytosis with neutrophilia of 80%, mild hepatic dysfunction, normal level of rheumatoid factor and antinuclear antibody, thrombocytopenia, elevated d-dimer and soluble interleukin2 receptor, extremely high serum ferritin (78 662 ng/mL), and splenomegaly. Although she had no arthritis or specific erythema, we made the diagnosis of AOSD according to Yamaguchi’s criteria with disseminated intravascular coagulation (DIC) and hemophagocytic syndrome (HPS) after ruling out infections, malignancies, or other connective tissue diseases. Twelve percent of AOSD patients have HPS. The mean serum ferritin of AOSD with HPS was reported at 18 179 ng/mL, which supported the diagnosis of AOSD because only a few other diseases could show such extremely high serum ferritin. Although she was treated with prednisolone (30 mg/day), her condition deteriorated and her left pleural effusion increased. Therefore, methylprednisolone 500 mg/day for 3 days was started followed by prednisolone 30 mg/day and immunosuppressive agent (Cyclosporine 50 mg/day), which improved her general condition, elevated C-reactive protein levels, and extremely high serum ferritin levels. CONCLUSIONS: We report the case of an elderly patient with severe AOSD, who developed HPS and DIC, whose extremely high serum ferritin level was useful in diagnosis. International Scientific Literature, Inc. 2017-12-06 /pmc/articles/PMC5726146/ /pubmed/29208852 http://dx.doi.org/10.12659/AJCR.905684 Text en © Am J Case Rep, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Articles Yamashita, Shun Furukawa, Naoko E. Matsunaga, Tomoyo Hirakawa, Yuka Tago, Masaki Yamashita, Shu-ichi Extremely High Serum Ferritin: An Instrumental Marker of Masquerading Adult-Onset Still’s Disease with Hemophagocytic Syndrome |
title | Extremely High Serum Ferritin: An Instrumental Marker of Masquerading Adult-Onset Still’s Disease with Hemophagocytic Syndrome |
title_full | Extremely High Serum Ferritin: An Instrumental Marker of Masquerading Adult-Onset Still’s Disease with Hemophagocytic Syndrome |
title_fullStr | Extremely High Serum Ferritin: An Instrumental Marker of Masquerading Adult-Onset Still’s Disease with Hemophagocytic Syndrome |
title_full_unstemmed | Extremely High Serum Ferritin: An Instrumental Marker of Masquerading Adult-Onset Still’s Disease with Hemophagocytic Syndrome |
title_short | Extremely High Serum Ferritin: An Instrumental Marker of Masquerading Adult-Onset Still’s Disease with Hemophagocytic Syndrome |
title_sort | extremely high serum ferritin: an instrumental marker of masquerading adult-onset still’s disease with hemophagocytic syndrome |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726146/ https://www.ncbi.nlm.nih.gov/pubmed/29208852 http://dx.doi.org/10.12659/AJCR.905684 |
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